홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

(S)-tert-butyl 5,6-di(nitrooxy)hexanoate → (S)-5,6-di(nitrooxy)hexanoic acid

HRID 1675998
노트
인쇄 미리보기

반응식

HRID 1675998 반응식
[N+:1]([O:4][C@H:5]([CH2:16][O:17][N+:18]([O-:20])=[O:19])[CH2:6][CH2:7][CH2:8][C:9]([O:11]C(C)(C)C)=[O:10])([O-:3])=[O:2]>C(Cl)Cl>[N+:1]([O:4][C@H:5]([CH2:16][O:17][N+:18]([O-:20])=[O:19])[CH2:6][CH2:7][CH2:8][C:9]([OH:11])=[O:10])([O-:3])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 59509520(S)-tert-butyl 5,6-di(nitrooxy)hexanoate

생성물 1

HCID 29923588(S)-5,6-di(nitrooxy)hexanoic acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
0 °C

실험 절차

To a solution of (S)-tert-butyl 5,6-di(nitrooxy)hexanoate (12.41 g, 42.155 mmol) in DCM (47 mL) cooled to 0° C. under N2, boron trifluoride diethyl ether complex (5.82 mL, 46.37 mmol) was added. The reaction mixture was stirred at 0° C. for 10 minutes and at rt for 3 hrs. The solution was washed with brine, the organic layer was separated, dried over sodium sulfate and concentrated under reduced pressure. The crude brown oil was used in the next step without further purification.

후처리

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  1. additionboron trifluoride diethyl ether complex (5.82 mL, 46.37 mmol) was added
  2. washThe solution was washed with brine
  3. customthe organic layer was separated
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe crude brown oil was used in the next step without further purification

출처 및 근거

ORD 기록
ord-24534e9923e848248099591fd173c9c3
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08003811B2

반응 노트

불러오는 중…